Evidence map›Paper›PMID 25158178›Full record

ArticleConnective tissue research2014

Correlation of ameloblastin with enamel mineral content.

John D Teepe, James E Schmitz, Yuanyuan Hu, Yoshihiko Yamada, Roberto J Fajardo, Charles E Smith, Yong-Hee P Chun

Abstract read
In one paragraph

Article in Connective tissue research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Functions of secretory calcium-binding phosphoproteins in dental mineralization.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Review
  2. Article
  3. Ameloblastin and its multifunctionality in amelogenesis: A review.Matrix biology : journal of the International Society for Matrix Biology · 2024
    Review
  4. Article
  5. Article
  6. ENAM mutations and digenic inheritance.Molecular genetics & genomic medicine · 2019
    Article
  7. Article
  8. Intrinsically disordered proteins and biomineralization.Matrix biology : journal of the International Society for Matrix Biology
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

John D TeepeDepartment of Periodontics, Dunn Dental Clinic, Lackland Air Force Base , San Antonio, TX , USA .
James E Schmitz
Yuanyuan Hu
Yoshihiko Yamada
Roberto J Fajardo
Charles E Smith
Yong-Hee P Chun

Funding

Oral and Craniofacial Development and DiseaseZIADE000720 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, YOSHIHIKO · 2009 to 2017
$6.1M
Role of ameloblastin for ameloblasts and enamel formationK08DE022800 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHUN, YONG-HEE PATRICIA · 2012 to 2016
$645k
A Shared MicroCT Instrument for Virtual Histology Imaging of Bone and Soft TissueS10RR025687 · NCRR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI FAJARDO, ROBERTO J · 2010 to 2010
$359k
NCRR NIH HHS S10 RR025687NIDCR NIH HHS K08 DE022800
6 · The paper itself

Abstract

In enamel formation, the deposition of minerals as crystallites starts when the mineralization front first forms at the start of the secretory stage. During maturation, the enamel layer accumulates significant amounts of new mineral as the crystallites grow in volume. Inversely related to mineral gain is loss of protein and water from the forming enamel. Both ameloblastin (Ambn) and enamelin are essential components for formation of a functional enamel layer. The aim of this study was to quantify the proportion of mineral and non-mineral material present in developing enamel relative to Ambn concentration using Ambn mutant mice mated with others overexpressing full-length Ambn from the mouse amelogenin promoter at lower (+), similar (++) or higher (+++) concentration than normal. Mandibular incisors (age: 7 weeks, n = 8) were imaged by micro-computed tomography and the enamel was analyzed from the apical region to the incisal edge in sequential 1.0 mm volumes of interest. Mineral density was determined using a series of hydroxyapatite (HA) phantoms to calibrate enamel density measurements. At the site where the mandibular incisor emerged into the oral cavity, the enamel volume, mineral weight, and mineral density were reduced when Tg Ambn was expressed at lower or higher levels than normal. While in wild-type the % mineral was >95%, it was negligible in Ambn-/-, 22.3% in Ambn-/-, Tg(+), 75.4% in Ambn-/-, Tg(++), and 45.2% in Ambn-/-, Tg(+++). These results document that the deposition of mineral and removal of non-mineral components are both very sensitive to expressed Ambn concentrations.

Indexed as

AmelogenesisAmelogeninAnimalsBone DensityDental EnamelIncisorMiceMice, KnockoutMicroscopy, Electron, ScanningX-Ray MicrotomographyAmelogeninAmeloblastinenamelenamel biomineralization/formationmicro-computed tomographymineralization frontmineralized tissue/development

Identifiers

PMID25158178
PMCPMC4471956

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.